Chromosome 13 Abnormality - CISMeF

" /> Chromosome 13 Abnormality - CISMeF

CISMeF

chu

Chromosome 13 AbnormalityNCIt concept

Preferred Label : Chromosome 13 Abnormality;

NCIt definition : An irregularity in the structure of chromosome 13.;

NCI Metathesaurus CUI : CL539335;

Details

Origin ID

C141237;

UMLS CUI

C4683646;

Currated CISMeF NLP mapping
- Anomaly of chromosome 13 [ORDO Disease]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Disease Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 13 [NCIt concept]

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29/04/2024

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